Canonical Allele Identifier: CA2637633102

Gene: TCAP

Linked Data

• gnomAD v4: 17-39666012-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39666013del , CM000679.2:g.39666013del	GRCh38
NC_000017.10:g.37822266del , CM000679.1:g.37822266del	GRCh37
NC_000017.9:g.35075792del	NCBI36
NG_008892.1:g.5668del , LRG_210:g.5668del
NG_042278.1:g.3033del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000309889.3:c.408del MANE Select	ENSP00000312624.2:p.Thr137GlnfsTer?
ENST00000309889.2:c.408del	ENSP00000312624.2:p.Thr137GlnfsTer?
ENST00000578283.1:c.336del	ENSP00000462787.1:p.Thr113GlnfsTer?
NM_003673.3:c.408del , LRG_210t1:c.408del	NP_003664.1:p.Thr137GlnfsTer?
NM_003673.4:c.408del MANE Select	NP_003664.1:p.Thr137GlnfsTer?